LDH info

Canonical Allele Identifier: CA16108157

Identifiers and link-outs to other resources

dbSNP Id: rs365060

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108959280C>G , CM000664.2:g.108959280C>G GRCh38
NC_000002.11:g.109575736C>G , CM000664.1:g.109575736C>G GRCh37
NC_000002.10:g.108942168C>G NCBI36
NG_008257.1:g.35093G>C

Transcript Alleles

HGVS Amino-acid change
NM_022336.3:c.-18-28248G>C (EDAR) VV NP_071731.1:p.=
XM_006712204.1:c.-18-28248G>C (EDAR) XP_006712267.1:p.=
XM_011510502.1:c.33+6343G>C (EDAR) XP_011508804.1:p.=
XM_011510503.1:c.33+6343G>C (EDAR) XP_011508805.1:p.=
XM_011510502.2:c.126+6343G>C (EDAR) XP_011508804.2:p.=
XM_011510503.2:c.126+6343G>C (EDAR) XP_011508805.2:p.=
XM_017004623.2:c.8370+186234C>G (RANBP2) XP_016860112.1:p.=
NM_022336.4:c.-18-28248G>C (EDAR) VV NP_071731.1:p.=
ENST00000258443.6:c.-18-28248G>C ENSP00000258443.2:p.=
ENST00000376651.1:c.-18-28248G>C ENSP00000365839.1:p.=
ENST00000409271.5:c.-134-18954G>C ENSP00000386371.1:p.=